Genomic structure and chromosomal localization of the human cathepsin O gene (CTSO)

Genomics

Volumn 53, Issue 2, 1998, Pages 231-234

  Santamaría, Iñigo ^a   Pendás, Alberto M ^a   Velasco, Gloria ^a   López Otín, Carlos ^a  

^a UNIVERSIDAD DE OVIEDO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CATHEPSIN; COMPLEMENTARY DNA; CYSTEINE PROTEINASE;

ARTICLE; BREAST CARCINOMA; CHROMOSOMAL LOCALIZATION; CHROMOSOME 4Q; EXON; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENOME; HUMAN; HUMAN CELL; INTRON; PRIORITY JOURNAL;

EID: 0032532144     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5180     Document Type: Article

References (24)

1. Ammar D. A., Eadie D. M., Wong D. J., Ma Y. Y., Kolakowski L. F., Yang-Feng T. L., Thompson D. A. Characterization of the human type 2 neuropeptide Y receptor gene (NPY2R) and localization to the chromosome 4q region containing the type 1 neuropeptide Y receptor gene. Genomics. 38:1996;392-398.
2. Anderson D. M., Johnson L., Glaccum M. B., Copeland N. G., Gilbert D. J., Jenkins N. A., Valentine V., Kirstein M. N., Shapiro D. N., Morris S. W., Grabstein K., Cosman D. Chromosomal assignment and genomic structure of IL-15. Genomics. 25:1995;701-706.
3. Berti P. J., Storer A. C. Alignment/phylogeny of the papain superfamily of cysteine proteases. J. Mol. Biol. 246:1995;273-283.
4. Buetow K. H., Murray J. C., Israel J. L., London W. T., Smith M., Kew M., Blanquet V., Brechot C., Redeker A., Govindarajah S. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc. Natl. Acad. Sci. USA. 86:1989;8852-8856.
5. Chauhan S. S., Popescu N. C., Ray D., Fleischmann R., Gottesman M. M., Troen B. R. Cloning, genomic organization and chromosomal localization of human cathepsin L. J. Biol. Chem. 268:1993;1039-1045.
6. Diriong S., Salehzada T., Bisbal C., Martinand C., Taviaux S. Localization of the ribonuclease L inhibitor gene (RNS4I), a new member of the interferon-regulated 2-5A pathway, to 4q31 by fluorescencein situ. Genomics. 32:1996;488-490.
7. Gelb B. D., Shi G. P., Chapman H. A., Desnick R. J. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science. 273:1996;1236-1238.
8. Giuili G., Roechel N., Scholl U., Mattei M. G., Guellaen G. Colocalization of the genes coding for the alpha 3 and beta 3 subunits of soluble guanylyl cyclase to human chromosome 4 at q31.3-q33. Hum. Genet. 91:1993;257-260.
9. Gong Q., Chan S. J., Bajkowski A. S., Steiner D. F., Frankfater A. Characterization of the cathepsin B gene and multiple mRNAs in human tissues: Evidence for alternative splicing of cathepsin B pre-mRNA. DNA Cell Biol. 12:1993;299-309.
10. Li L., Kaplan J. Characterization of yeast methyl sterol oxidase (ERG25) and identification of a human homologue. J. Biol. Chem. 271:1996;16927-16933.
11. Lin A. E., Garver K. L., Diggans G., Clemens M., Wenger S. L., Steele M. W., Jones M. C., Israel J. Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes. Am. J. Med. Genet. 31:1988;533-548.
12. Mills K. A., Mathews K. D., Scherpbier T. H., Buetow K. H., Baldini A., Ballabio A., Borsani G. Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. Genomics. 36:1996;374-376.
13. Morrison N., Harrap S. B., Arriza J. L., Boyd E., Connor J. M. Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1. Hum. Genet. 85:1990;130-132.
14. Pendás A. M., Matilla T., Uría J. A., Freije J. P., Fueyo A., Estivill X., López-Otín C. Mapping of the human Zn-alpha 2-glycoprotein gene (AZGP1) to chromosome 7q22 by in situ hybridization. Cytogenet. Cell Genet. 66:1994;263-266.
15. Rao N. V., Rao G. V., Hoidal J. R. Human dipeptidyl-peptidase I: Gene characterization, localization, and expression. J. Biol. Chem. 272:1997;10260-10265.
16. Ratajczak T., Woollatt E., Kumar P., Ward B. K., Minchin R. F., Baker E. Cyclophilin 40 (PPID) gene map position 4q31.3. Chromosome Res. 5:1997;151.
17. Rood J. A., Van Horn S., Drake F. H., Gowen M., Debouck C. Genomic organization and chromosome localization of the human cathepsin K gene (CTSK). Genomics. 41:1997;169-176.
18. Sarda P., Lefort G., Fryns J. P., Humeau C., Rieu D. Interstitial deletion of the distal long arm of chromosome 4. J. Med. Genet. 29:1992;259-261.
19. Shi G., Webb A. C., Karen A. F, Knoll J. H. M., Lemere C. A., Munger J. S., Chapman H. A. Human cathepsin S: Chromosomal localization, gene structure, and tissue distribution. J. Biol. Chem. 269:1994;11530-11536.
20. Sun W., Ferrer-Montiel A. V., Schinder A. F., McPherson J. P., Evans G. A., Montal M. Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors. Proc. Natl. Acad. Sci. USA. 89:1992;1443-1447.
21. Terman B. I., Jani-Sait S., Carrion M. E., Shows T. B. The KDR gene maps to human chromosome 4q31.2-q32, a locus which is distinct from locations for other type III growth factor receptor tyrosine kinases. Cytogenet. Cell Genet. 60:1992;214-215.
22. Velasco G., Ferrando A. A., Puente X. A., Sánchez L. M., López-Otín C. Human cathepsin O: Molecular cloning from a breast carcinoma, production of the active enzyme in Escherichia coli, and expression analysis in human tissues. J. Biol. Chem. 269:1994;27136-27142.
23. Wang X., Chan S. J., Eddy R. I., Byers M. G., Fukushima Y., Henru W. M., Haley I. I., Stelner D. F., Shows T. B. Chromosome assignment of cathepsin B (CTSB) to 8p22 and cathepsin H (CTSH) to 15q24-q25. Cytogen. Cell Genet. 46:1987;710-711.
24. Wanschura S., Schoenmakers E. F., Huysmans C., Bartnitzke S., Van de Ven W. J., Bullrdiek J. Mapping of the human HMG2 gene to 4q31. Genomics. 31:1996;264-265.